Dr Vampa S.R.L.

Dr Vampa S.R.L. specializes in portable examination and treatment room lighting systems. These devices are designed to provide adjustable, high-intensity illumination specifically for medical environments, ensuring clear visibility during clinical procedures in compact or mobile settings.

Dr Vampa S.R.L. is based in the United States. The company’s location is relevant for understanding its regulatory context and market focus.

Dr Vampa S.R.L.’s devices fall under Class I classification, which typically means they pose minimal risk and are subject to the lowest level of regulatory oversight. This classification is determined based on factors like the device’s intended use, duration of contact with the body, and potential for harm.

Yes, Dr Vampa S.R.L.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices in the U.S. market, ensuring transparency and traceability for regulatory and clinical purposes.